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Difluoromethane → 2-Difluoromethylthio-5-pyrid-2-yl-1,3,4-thiadiazole

HRID 329943
ノート
印刷プレビュー

反応式

HRID 329943 の反応式
[SH:1][C:2]1[S:3][C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)=[N:5][N:6]=1.[OH-].[K+].[F:15][CH2:16][F:17]>O1CCOCC1.O.[I-].[K+].[Br-].C([NH+](CCCC)CCCC)CCC>[F:15][CH:16]([F:17])[S:1][C:2]1[S:3][C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)=[N:5][N:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 3

HCID 6345DifluoromethaneHCID 14797Potassium HydroxideHCID 178527949HCID 178527949、化合物

生成物 1

HCID 198704882-Difluoromethylthio-5-pyrid-2-yl-1,3,4-thiadiazole収率 75.1%

試薬・触媒・溶媒 4

HCID 4875Potassium Iodide触媒HCID 13798051Tributylammonium bromide
触媒
HCID 962Water溶媒
HCID 312751,4-Dioxane溶媒

実験手順

A suspension of 341.5 g (l.75 mol) of 2-mercapto-5-pyrid-2-yl-1,3,4-thiadiazole in 4000 ml of dioxane is added to a solution of 230.5 g of 85% potassium hydroxide in 800 ml of water. Then 10 g of potassium iodide and 6 g of tributylammonium bromide are added to the reaction mixture and 750 g (~8.6 mol) of gaseous difluoromethane are introduced over 41/2 hours at 22°-37° C. After evaporating off the dioxane, the reaction mixture is diluted with ethyl acetate, the aqueous phase is separated and the organic solution is washed cold with 1N sodium hydroxide and water, dried over sodium sulfate and clarified with activated carbon. They ethyl acetate is removed under vacuum and the residue is crystallised from ethyl acetate/hexane, affording 321.9 g (75.1%) of the title compound with a melting point of 90°-92° C.

後処理

  1. additionare introduced over 41/2 hours at 22°-37° C
  2. customAfter evaporating off the dioxane
  3. additionthe reaction mixture is diluted with ethyl acetate
  4. customthe aqueous phase is separated
  5. washthe organic solution is washed cold with 1N sodium hydroxide and water
  6. dry with materialdried over sodium sulfate
  7. customThey ethyl acetate is removed under vacuum
  8. customthe residue is crystallised from ethyl acetate/hexane

出典と根拠

ORDレコード
ord-9ec7e6f0f65c41ab83ae5aecb742d22c
出典データセット
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04894380

反応ノート

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